Canonical Allele Identifier: PA2826566707
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 140801
ClinVar RCV Id: RCV000128975 RCV000417795 RCV000423419 RCV000435449 RCV000427068 RCV000428004 RCV000429076 RCV000436530 RCV000444430 RCV000472876 RCV000418811 RCV000427674 RCV000437920 RCV000439333 RCV000785510 RCV001582600 RCV002288619
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Cys102Tyr
CA000174
NM_001276761.3:c.305G>A